Radiopharma QA Specialist — GMP & CAPA Leader
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Quality Assurance - QA/QC
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Healthcare
Job Description & How to Apply Below
Siemens Healthineers AG is seeking a Quality Specialist to oversee a US-based site manufacturing radioactive sterile injectables under 21 CFR Part 212 and USP 825. You will lead GMP investigations, CAPA programs, batch release reviews, and audits to ensure regulatory compliance and product quality.
The role emphasizes on-site training, mentoring, data integrity reviews, and collaboration with FDA inspections. Flexibility to travel and strong pharmaceutical QA background are preferred.
Are you ready to take on the Radiopharma QA Specialist — GMP & CAPA Leader role at Siemens Healthineers AG?
This role, Radiopharma QA Specialist — GMP & CAPA Leader at Siemens Healthineers AG, could be your next career step.
We would love to welcome a new Radiopharma QA Specialist — GMP & CAPA Leader to our group in Covington, LA, United States.
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